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"Lina" endoscope defogging wipe - Taiwan Registration 2f4705c6cd8608e0e25365b1c7c535af

Access comprehensive regulatory information for "Lina" endoscope defogging wipe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f4705c6cd8608e0e25365b1c7c535af and manufactured by LiNA Medical Polska sp.z.o.o.;; LINA MEDICAL APS. The authorized representative in Taiwan is Huizhong Co., Ltd.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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2f4705c6cd8608e0e25365b1c7c535af
Registration Details
Taiwan FDA Registration: 2f4705c6cd8608e0e25365b1c7c535af
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Device Details

"Lina" endoscope defogging wipe
TW: โ€œๅˆฉๆ‹ฟโ€ๅ…ง่ฆ–้ก้™ค้œงๆ‹ญ็ด™
Risk Class 2

Registration Details

2f4705c6cd8608e0e25365b1c7c535af

DHA00602061305

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Feb 26, 2010

Feb 26, 2025